Stereoselective synthesis of conjugated all-trans-tetraenes. Application to the synthesis of β-parinaric acid methyl ester
作者:Guy Solladié、Chakib Kalaï、Marc Adamy、Françoise Colobert
DOI:10.1016/s0040-4039(97)01594-3
日期:1997.9
in this paper is reported the stereoselective synthesis of all-trans-tetraenes by reductive elimination of 1,8-dibenzoate-2,4,6-trienes with sodium amalgam. The method was applied to the syntheses of 4E, 6E, 8E, 10E-heptatetraene and β—parinaric acid methyl ester.
本文报道了通过汞齐钠还原消除1,8-二苯甲酸酯-2,4,6-三烯的立体选择性合成全反式四烯的方法。该方法适用于4E,6E,8E,10E-庚二烯和β-二十二烷酸甲酯的合成。